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A Phase II Trial of Sofosbuvir (SOF) and GS-5816 for People With Chronic Hepatitis C Virus Infection and Recent Injection Drug Use (SIMPLIFY)

26. februar 2019 opdateret af: Kirby Institute

A Phase II, Open-label, Single Arm, Multicentre, International Trial of Sofosbuvir (SOF) and GS-5816 for People With Chronic Hepatitis C Virus Infection and Recent Injection Drug Use

To evaluate the proportion of patients with undetectable HCV RNA at 12 weeks post end of treatment (SVR12) following sofosbuvir/GS-5816 therapy for 12 weeks in people with chronic HCV infection and recent injection drug use.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

103

Fase

  • Fase 2

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • New South Wales
      • Sydney, New South Wales, Australien, 2052
        • The Kirby Institute

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  1. Participants have voluntarily signed the informed consent form.
  2. 18 years of age or older.
  3. Chronic HCV infection as defined by anti-HCV antibody or HCV RNA detection for greater than 6 months.
  4. HCV RNA plasma ≥ 1000 IU/ml at Screening.
  5. HCV genotypes 1-6.
  6. Recent injecting drug use (previous 6 months).
  7. Compensated liver disease.
  8. Participants with Fibroscan >12 KPa or AFP >50 ng/mL must have an abdominal ultrasound or CT scan without evidence of hepatocellular carcinoma within 2 months prior to screening.
  9. Negative pregnancy test at baseline (females of childbearing potential only).
  10. All fertile males and females must be using effective contraception during treatment and during the 30 days after treatment end.

Exclusion Criteria:

  1. History of any of the following:

    1. Clinically significant illness (other than HCV) or any other major medical disorder that may interfere with the participant treatment, assessment or compliance with the protocol; participants currently under evaluation for a potentially clinically significant illness (other than HCV) are also excluded.
    2. Clinical hepatic decompensation (i.e. ascites, encephalopathy or variceal haemorrhage)
    3. Solid organ transplant
    4. Malignancy within 5 years prior to screening, with exception of specific cancers that may have been cured by surgical resection (basal cell skin cancer, etc.). Subjects under evaluation for possible malignancy are also excluded.
    5. Significant drug allergy (such as anaphylaxis or hepatotoxicity).
  2. Screening ECG with clinically significant abnormalities
  3. Any of the following lab parameters at screening:

    1. ALT > 10 x ULN
    2. AST > 10 x ULN
    3. Direct bilirubin > 1.5 x ULN
    4. Platelets < 50,0000/μL
    5. HbA1c > 8.5%
    6. Creatinine clearance (CLcr) < 60 mL/min
    7. Haemoglobin < 11 g/dL for females ; < 12 g/dL for males
    8. Albumin < 30g/L
    9. INR > 1.5 ULN unless subject has known haemophilia or is stable on an anticoagulant regimen affecting INR
  4. Pregnant or nursing female.
  5. HIV infection or HBV infection (HBcAb and HBsAg positive)
  6. Use of prohibited concomitant medications as described in section 5.2
  7. Chronic use of systemically administered immunosuppressive agents (e.g. prednisone equivalent > 10 mg/day)
  8. Known hypersensitivity to GS-5816, sofosbuvir (SOF) or formulation excipients.
  9. Therapy with any anti-neoplastic or immunomodulatory treatment (including supraphysiologic doses of steroids and radiation) ≤6 months prior to the first dose of study drug.
  10. Any investigational drug ≤6 weeks prior to the first dose of study drug.
  11. Previous therapy with sofosbuvir (SOF) or an NS5A inhibitor prior to the first dose of study drug.
  12. Ongoing severe psychiatric disease as judged by the treating physician.
  13. Frequent injecting drug use that is judged by the treating physician to compromise treatment safety.
  14. Inability or unwillingness to provide informed consent or abide by the requirements of the study.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Sofosbuvir (SOF)/GS-5816
12 weeks of Sofosbuvir (SOF)/GS-5816 (400mg/100mg) in an oral once-daily fixed dose combination
12 weeks of Sofosbuvir (SOF)/GS-5816 (400mg/100mg) in an oral once-daily fixed dose
Andre navne:
  • SOF/GS-5816

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Sustained Virological Response (SVR12)
Tidsramme: Week 24
To evaluate the proportion of patients with undetectable HCV RNA at 12 weeks post end of treatment (SVR12) following sofosbuvir (SOF)/GS-5816 therapy for 12 weeks in people with chronic HCV infection and recent injection drug use.
Week 24

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Behandlingsadhærens
Tidsramme: Baseline til uge 12
For at evaluere andelen af ​​patienter, der følger terapien (både overholdelse af behandlingen og afbrydelse af behandlingen)
Baseline til uge 12
Impact of adherence on therapy (association between adherence and response to treatment )
Tidsramme: early (0-3 weeks), mid (4-7 weeks) and late (8-11 weeks) during therapy
To evaluate the association between adherence and response to treatment [including an evaluation of the impact of early (0-3 weeks), mid (4-7 weeks) and late (8-11 weeks) missed doses on response to therapy]; Adehernce will be measure via a self report quesitonanire and pill counts via return of the weeekly blister packs. The impact of the number and timing of missed pills will be evaluated.
early (0-3 weeks), mid (4-7 weeks) and late (8-11 weeks) during therapy
Factors associated with on-treatment adherence
Tidsramme: Baseline to Week 12
To evaluate factors associated with on-treatment adherence >90% and treatment discontinuation. Demographic and behavioural factors will be examined.
Baseline to Week 12
End of Treatment Response (ETR) (proportion of participants with undetectable HCV RNA at the end of treatment (ETR)
Tidsramme: Week 12
To evaluate the proportion of participants with undetectable HCV RNA at the end of treatment (ETR)
Week 12
Safety and tolerability (number and type of adverse events and serious adverse events)
Tidsramme: Baseline to Week 24
To evaluate the number and type of adverse events and serious adverse events on treament and for 12 weeks post end of treatment
Baseline to Week 24
Change in drug use
Tidsramme: Baseline to Week 12
To evaluate the change in drug use during treatment
Baseline to Week 12
Change in mental health
Tidsramme: Basleine to Week 12
To evaluate the change in mental health during treatment
Basleine to Week 12
Change in health related quality of life
Tidsramme: Baseline to Week 12
To evaluate the change in health-related quality of life during treatment
Baseline to Week 12
Impact of mixed infection on treatment response
Tidsramme: Baseline to Week 24
To evaluate the rate of mixed HCV infection at baseline and among those with treatment non-response
Baseline to Week 24
Reinfection Rate
Tidsramme: Week 108
To evaluate the rate of HCV reinfection during and up to two years following treatment
Week 108
Immunovirological factors associated with treatment clearance
Tidsramme: Week 24
To evaluate immunovirological factors associated with treatment clearance. We will evaluate cytokines and chemokines (e.g. interferon inducible protein 10), T-cell responses, viral evolution and genetic markers (e.g. inteferon lambda 4) that are potentially associated with treatment induced clearance
Week 24
Utility of Dried Blood Spot (DBS) (method for monitoring HCV including treatment response)
Tidsramme: Week 108
To evaluate the utility of dried blood spot (DBS) as a simple method for monitoring HCV including treatment response. HCV RNA will be measured from DBS samples and then compared to HCV RNA levels measured using standard methods (EDTA Plasma samples and Roche Taqman)
Week 108

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Efterforskere

  • Ledende efterforsker: Greg Dore, MBBS PhD, Kirby Institute

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

16. marts 2016

Primær færdiggørelse (Faktiske)

17. april 2017

Studieafslutning (Faktiske)

28. november 2018

Datoer for studieregistrering

Først indsendt

4. januar 2015

Først indsendt, der opfyldte QC-kriterier

7. januar 2015

Først opslået (Skøn)

12. januar 2015

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

27. februar 2019

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

26. februar 2019

Sidst verificeret

1. februar 2019

Mere information

Begreber relateret til denne undersøgelse

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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